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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363356생성일: 2026년 10월 25일

Hydrazine, acetate (1:1) → 2,3-di-O-acetyl-4,6-dichloro-4,6-dideoxy-D-galactopyranose

https://huagongshe.com/reaction/363356

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참여 물질

역할이름HCID투입량
반응물Hydrazine, acetate (1:1)HCID 165591—
반응물acetyl 2, 3-di-O-acetyl-4,6-dichloro-4,6-dideoxy-D-galactopyranoseHCID 131721128—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2,3-di-O-acetyl-4,6-dichloro-4,6-dideoxy-D-galactopyranoseHCID 53747013105.8%

반응 단계

A solution of acetyl 2,3-di-O-acetyl-4,6-dichloro-4,6-dideoxy-D-galactopyranose (compound 82) (2.24 g, 6.5 mmol) and hydrazine acetate (903 mg) in DMF (22 mL) was stirred for 2 hours at room temperature. The reaction mixture was then diluted with dichloromethane (250 mL) and washed 4 times with water (4×250 mL), dried over anhydrous sodium sulfate and evaporated. Flash chromatography using hexane-ethyl acetate (1:1) as an eluent gave 2,3-di-O-acetyl-4,6-dichloro-4,6-dideoxy-D-galactopyranose (~6.88 mmol). This compound was then dissolved in dichloromethane (20 mL) cooled to 0° C., and trichloroacetonitrile (3.35 mL, 34.4 mmol) was added. After stirring at 0° C. for 40 minutes, the solvent was evaporated and the residue was chromatographed on a silica gel column, eluting with hexane-ethyl acetate (5:1), to give imidate 83 (1.14 g, 39%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05874411
출처 데이터셋uspto-grants-1999_02
ORD IDord-9159116249ce423c9bdce983b932fca8
출처 메모uspto-grants-1999_02